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Q33383191-58CE00C9-BB0A-4B35-9C6E-48D170208C86
Q33383191-58CE00C9-BB0A-4B35-9C6E-48D170208C86
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Statement
http://www.wikidata.org/entity/statement/Q33383191-58CE00C9-BB0A-4B35-9C6E-48D170208C86
Mecp2-null mice provide new neuronal targets for Rett syndrome.
P2860
Q33383191-58CE00C9-BB0A-4B35-9C6E-48D170208C86
BestRank
Statement
http://www.wikidata.org/entity/statement/Q33383191-58CE00C9-BB0A-4B35-9C6E-48D170208C86
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wasDerivedFrom
ab002bd767310d96a9bd16b4a3f4759af7008cc9
P2860
MeCP2 deficiency in Rett syndrome causes epigenetic aberrations at the PWS/AS imprinting center that affects UBE3A expression